The secretome atlas of two mouse models of progeria

Hutchinson‐Gilford progeria syndrome (HGPS) is a rare genetic disease caused by nuclear envelope alterations that lead to accelerated aging and premature death. Several studies have linked health and longevity to cell‐extrinsic mechanisms, highlighting the relevance of circulating factors in the agi...

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Detalles Bibliográficos
Autores principales: Quintana‐Torres, Diego, Valle‐Cao, Alejandra, Bousquets‐Muñoz, Pablo, Freitas‐Rodríguez, Sandra, Rodríguez, Francisco, Lucia, Alejandro, López‐Otín, Carlos, López‐Soto, Alejandro, Folgueras, Alicia R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577534/
https://www.ncbi.nlm.nih.gov/pubmed/37565451
http://dx.doi.org/10.1111/acel.13952

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577534/
https://www.ncbi.nlm.nih.gov/pubmed/37565451
http://dx.doi.org/10.1111/acel.13952

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